Author:
Baris Savas,Boluk Selime Ozen
Subject
Immunology,Immunology and Allergy
Reference18 articles.
1. Immunodeficiency, centromeric heterochromatin instability of chromosomes 1, 9, and 16, and facial anomalies: the ICF syndrome;Maraschio;J. Med. Genet.,1988
2. The gene mutations and subtelomeric DNA methylation in immunodeficiency, centromeric instability and facial anomalies syndrome;Hu;Autoimmunity.,2019
3. DNMT3B deficiency presenting as severe combined immune deficiency: a case report;Mehawej;Clin. Immunol.,2020
4. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome;Hansen;Proc. Natl. Acad. Sci. U. S. A.,1999
5. Three novel ZBTB24 mutations identified in Japanese and Cape Verdean type 2 ICF syndrome patients;Nitta;J. Hum. Genet.,2013